Colon Cancer: Gene >> CCNH

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000256897
Start	87411258:87411258(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.206C>T
AA Mutation	p.Ser69Leu(p.S69L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000256897
Start	87408122:87408122(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs568535217
CDS Mutation	c.379G>A
AA Mutation	p.Gly127Arg(p.G127R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000256897
Start	87401730:87401730(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.732C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000256897
Start	87401756:87401756(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755370075
CDS Mutation	c.706C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> CCNH

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000256897
Start	87409356:87409356(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.248C>T
AA Mutation	p.Ala83Val(p.A83V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000256897
Start	87404887:87404890(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.643_646delACTG
AA Mutation	p.Thr215ProfsTer21(p.T215Pfs*21)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript